𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Diastereoselectivity in the intramolecular diels-alder reaction of dienylpropynoates

✍ Scribed by David H. Birtwistle; John M. Brown; Michael W. Foxton


Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
892 KB
Volume
44
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Intramolecular Diels-Alder reaction of s
✍ Masahito Segi; Mamoru Takahashi; Tadashi Nakajima; Sohei Suga; Shinji Murai; Nob πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 234 KB

Intramolecular Diels-Alder reaction of selenoaldehydes which were generated from bis(trimethylsily1) selenide and dienals gave the corresponding bicyclic adducts.

Intramolecular diels-alder reactions of
✍ George A. Kraus; Jeff Raggon; P.J. Thomas; Dan Bougie πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 209 KB

The first examples of intramolecular Diels-Alder reactions on indoles indicate that this reaction may be employed for the direct preparation of highly functionalized dihydroindoles. The hybridization of the atoms in the tether plays a crucial role.

The intramolecular cation radical diels-
✍ Bijan Harirchian; Nathan L Bauld πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 French βš– 181 KB

The first examples of intramolecular cation radical Die&-Alder reactions have been established using trienes which cyclize to hydroindane systems. The extremely high endo stereoselectivity characteristic of the cation radical Diels-Alder reaction is effectively exploited to generate trans-hydroinda